RS863224906 OPA1

Health Risk Chr 3:193657197
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal dominant optic atrophy classic form
OPA1-related disorder
Optic atrophy
Autosomal dominant optic atrophy classic form
OPA1-related disorder
Optic atrophy
Other Variants in OPA1
rs28939082 rs879255510 rs80356530 rs879255560 rs121908375 rs104893753 rs879255511 rs879255512 rs80356531 rs121908376
Ask Dr. Hemsworth about this variant